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- W4382982649 abstract "Abstract An unprecedented cascade Michael/cyclization reaction of 4‐chromanone derivatives, aldehydes, and 2‐cyanothioacetamide was presented for the preparation of distinctive 2‐amino‐4‐aryl‐5 H ‐chromeno[4,3‐ b ]pyridine‐3‐carbonitriles promoted by ammonium acetate. The optimized reaction conditions were used for the synthesis of 2‐amino‐4‐aryl‐5 H ‐chromeno[4,3‐ b ]pyridine‐3‐carbonitrile derivatives in medium to high yields. The synthetic method features a convenient operational process, easy access to raw material as well as high atom economy." @default.
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- W4382982649 date "2023-07-02" @default.
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- W4382982649 title "Facile access to <scp>2‐amino‐4‐aryl‐5</scp><i>H</i>‐chromeno[4,3‐<i>b</i>]pyridine‐3‐carbonitriles through a strategy of one‐pot Michael/cyclization reaction" @default.
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- W4382982649 doi "https://doi.org/10.1002/jhet.4704" @default.
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